The Evidence for Association of ATP2B2 Polymorphisms with Autism in Chinese Han Population

PLoS ONE

Volumn 8, Issue 4, 2013, Pages

  Yang, Wen ^a,b   Liu, Jing ^a,b   Zheng, Fanfan ^a,b   Jia, Meixiang ^a,b   Zhao, Linnan ^a,b   Lu, Tianlan ^a,b   Ruan, Yanyan ^a,b   Zhang, Jishui ^c   Yue, Weihua ^a,b   Zhang, Dai ^a,b,d   Wang, Lifang ^a,b  

^a BEIJING HOSPITAL   (China)

^b PEKING UNIVERSITY SIXTH HOSPITAL   (China)

^c CAPITAL MEDICAL UNIVERSITY   (China)

^d Tsinghua University   (China)

Author keywords

[No Author keywords available]

Indexed keywords

PLASMA MEMBRANE CALCIUM TRANSPORTING ADENOSINE TRIPHOSPHATASE;

ADOLESCENT; ALLELE; ARTICLE; ATPASE CALCIUM TRANSPORTING PLASMA MEMBRANE 2 GENE; AUTISM; CHILD; CHINESE; CONTROLLED STUDY; DNA SEQUENCE; FAMILIAL DISEASE; FEMALE; GENE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC SCREENING; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHINA; ETHNIC GROUPS; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; PLASMA MEMBRANE CALCIUM-TRANSPORTING ATPASES; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84876442861     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0061021     Document Type: Article

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